Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00828945
Other study ID # A2581178
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 2009
Est. completion date March 2011

Study information

Verified date February 2021
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

It is a prospective observational study. Patients will be high risk patients (for developing cardiovascular events) that are treated with a statin. Patients will be enrolled at a normal clinic visit and provided with a small box containing info about the disease, a LDL self-test and two questionnaires. They will test themselves for LDL at home between normal clinic visits (normally 12 months interval) and note their value. In the end of the study all patients will fill out a questionnaire with questions if the tests and info have raised their awareness of the disease as well if their motivation to be compliant has increased. We want to look at the possibility to put more responsibility for treatment and for reaching treatment goals on the patients since there's a big problem with compliance in this group of patients.


Description:

Consecutive patient sampling


Recruitment information / eligibility

Status Completed
Enrollment 259
Est. completion date March 2011
Est. primary completion date March 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Aged 18 years or older and able to understand and sign the informed consent form. - Patients diagnosed with hyperlipidemia and a very high risk developing cardiovascular disease prescribed statin treatment according to clinical praxis and the recommendations set forth in the MPA national guideline for treatment of hyperlipidemia. Exclusion Criteria: - Patients contraindicated for statin treatment according to market authorization for these drugs should be excluded from the study. - Patients participating in other clinical trials or non-interventional studies.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Lipid Self Test
Self test for lipid levels, twice during study period

Locations

Country Name City State
Sweden Pfizer Investigational Site Akersberga
Sweden Pfizer Investigational Site Forshaga
Sweden Pfizer Investigational Site Goteborg
Sweden Pfizer Investigational Site Goteborg
Sweden Pfizer Investigational Site Goteborg
Sweden Pfizer Investigational Site Hoganas
Sweden Pfizer Investigational Site Jonkoping
Sweden Pfizer Investigational Site Lessebo
Sweden Pfizer Investigational Site Lilla Edet
Sweden Pfizer Investigational Site Limhamn
Sweden Pfizer Investigational Site Malmo
Sweden Pfizer Investigational Site Oviken
Sweden Pfizer Investigational Site Partille
Sweden Pfizer Investigational Site Stockholm
Sweden Pfizer Investigational Site Taby
Sweden Pfizer Investigational Site Trollhattan
Sweden Pfizer Investigational Site Vasteras

Sponsors (1)

Lead Sponsor Collaborator
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Participants With Positive Response on Increased Motivation Using a Self-test at Month 12 Participants with "Yes" response to a question which stated "The self-test have increased my motivation for taking my medication for hyperlipidemia?". The self test done for assessment of LDL levels using CARE diagnostica LDL-cholesterol test. Month 12
Primary Percentage of Participants With Positive Response on Increased Motivation After Awareness at Month 12 Participants with "Yes" response to a question which stated "The awareness of my disease has increased my motivation for taking my medication for hyperlipidemia?". Month 12
Primary Percentage of Participants With Positive Response on Self-estimated Treatment Compliance at Week 8 Participants with "Yes" response to a question which stated "Have you been taking at least 90% of your medication for hyperlipidemia?". Week 8
Primary Percentage of Participants With Positive Response on Self-estimated Treatment Compliance at Month 6 Participants with "Yes" response to a question which stated "Have you been taking at least 90% of your medication for hyperlipidemia?". Month 6
Primary Percentage of Participants With Positive Response on Self-estimated Treatment Compliance at Month 12 Participants with "Yes" response to a question which stated "Have you been taking at least 90% of your medication for hyperlipidemia?". Month 12
Primary Percentage of Participants With LDL Lower Than 2.5 mmol/L at Week 8 LDL levels were self-assessed by participants using CARE diagnostica LDL-cholesterol test. Week 8
Primary Percentage of Participants With LDL Lower Than 2.5 mmol/L at Month 6 LDL levels were self-assessed by participants using CARE diagnostica LDL-cholesterol test. Month 6
Primary Percentage of Participants With LDL Lower Than 2.5 mmol/L at Month 12 LDL levels were self-assessed by participants using CARE diagnostica LDL-cholesterol test. Month 12
Primary Percentage of Participants With Response Achieving Targeted LDL-cholesterol Level at Week 8 Participants with "Yes" or "No" responses to a question which stated "Have you reached your target LDL-cholesterol level?". LDL levels were self-assessed by participants using CARE diagnostica LDL-cholesterol test. Week 8
Primary Percentage of Participants With Response Achieving Targeted LDL-cholesterol Level at Month 6 Participants with "Yes" or "No" responses to a question which stated "Have you reached your target LDL-cholesterol level?". LDL levels were self-assessed by participants using CARE diagnostica LDL-cholesterol test. Month 6
Primary Percentage of Participants With Response Achieving Targeted LDL-cholesterol Level at Month 12 Participants with "Yes" or "No" responses to a question which stated "Have you reached your target LDL-cholesterol level?". LDL levels were self-assessed by participants using CARE diagnostica LDL-cholesterol test. Month 12
See also
  Status Clinical Trial Phase
Completed NCT00001154 - Lipoprotein Metabolism in Normal Volunteers and Patients With High Levels of Lipoproteins
Completed NCT02927184 - Safety and Tolerability of VK2809 in Patients With Primary Hypercholesterolemia and Non-Alcoholic Fatty Liver Disease Phase 2
Completed NCT04640012 - Ascending-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics of DC371739 Single-Dose Treatment in Healthy Subjects Phase 1
Completed NCT03213288 - Bilberry Fruit and Black Rice Derived Anthocyanins on Lipid Status N/A
Completed NCT00382564 - Magnetic Resonance Angiography to Diagnose Atherosclerotic Disease N/A
Recruiting NCT02979704 - A Comparative Study of Rosuvastatin and Atorvastatin in Patients With Hyperlipidemia Phase 2/Phase 3
Completed NCT02569814 - A Study to Compare the Pharmacokinetics and Safety of a Fixed Dose Combination of Fimasartan/Amlodipine/Rosuvastatin Phase 1
Completed NCT02428998 - Safety for 24 Weeks Intake of Korean Red Ginseng in Adults N/A
Completed NCT02280590 - Comparison of the Efficacy and Safety of Cresnon® and Crestor® in Patients With Hyperlipidemia Phase 4
Completed NCT01678183 - Financial Incentives for Medication Adherence N/A
Completed NCT01694446 - Regulation of Intestinal and Hepatic Lipoprotein Production by Glucose and Fructose N/A
Completed NCT01426412 - A Study of LY3015014 in Healthy Participants With Elevated Low Density Lipoprotein Cholesterol Phase 1
Completed NCT01131832 - Genetic Basis for Heterogeneity in Response of Plasma Lipids to Plant Sterols Phase 4
Completed NCT00534105 - Lipid Metabolism in Gestational Diabetes N/A
Completed NCT00758303 - A Study to Evaluate the Lipid Regulating Effects of TRIA-662 Phase 2/Phase 3
Recruiting NCT00408824 - Investigation of Genetic Risk of Metabolic Syndrome in Company Employee (NGK Study) N/A
Terminated NCT00299169 - Randomized Trial Comparing N of 1 Trials to Standard Practice to Improve Adherence to Statins in Patients With Diabetes Phase 4
Completed NCT00362206 - Comparison of the Combination of Fenofibrate and Simvastatin Versus Pravastatin Phase 3
Completed NCT00381992 - Risk Assessment of Long-Haul Truck Drivers N/A
Completed NCT00414986 - Using Learning Teams for Reflective Adaptation for Diabetes and Depression N/A